A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1269n100



Internal ID20152885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102116359..102385022hg38UCSC Ensembl
chr11:101987090..102255753hg19UCSC Ensembl
chr11:101492300..101760963hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38268664
hg19268664
hg18268664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051735, nsv1052348, nsv1050961
Samples
Known GenesBIRC2, BIRC3, YAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1269n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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